This compound is miscible in water at a concentration of 50 µl/mL or approximately 47 µg/mL, based on a density of 0.935 g/mL. Solubility in other solvents, such as DMSO, has not been determined.
D183601
2,5-Dimethylpyrrole
98%
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About This Item
Formule empirique (notation de Hill):
C6H9N
Numéro CAS:
Poids moléculaire :
95.14
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
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Produits recommandés
Niveau de qualité
Essai
98%
Forme
liquid
Indice de réfraction
n20/D 1.505 (lit.)
pb
165 °C/740 mmHg (lit.)
Densité
0.935 g/mL at 25 °C (lit.)
Chaîne SMILES
Cc1ccc(C)[nH]1
InChI
1S/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
Clé InChI
PAPNRQCYSFBWDI-UHFFFAOYSA-N
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Catégories apparentées
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
129.2 °F - closed cup
Point d'éclair (°C)
54 °C - closed cup
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Les clients ont également consulté
Ireneusz Nowak et al.
Organic letters, 5(18), 3345-3348 (2003-08-29)
[reaction: see text] Protection of the amino group of adenine and guanine nucleosides was effected by heating the substrates in 2,5-hexanedione. The resulting 2,5-dimethylpyrrole adducts were stable toward bases but were hydrolyzed with TFA/H(2)O to regenerate the amino function.
Hongyin Yin et al.
PloS one, 8(9), e76011-e76011 (2013-10-08)
The formation of pyrrole adducts might be responsible for peripheral nerve injury caused by n-hexane. The internal dose of pyrrole adducts would supply more information for the neurotoxicity of n-hexane. The current study was designed to investigate the tissue distributions
Joseph M Beames et al.
The Journal of chemical physics, 131(17), 174305-174305 (2009-11-10)
The photophysical properties of porphyrins have relevance for their use as light-activated drugs in cancer treatment and sensitizers in solid-state solar cells. However, the appearance of their UV-visible spectra is usually explained inadequately by qualitative molecular-orbital theories. We intend to
Xianjie Li et al.
Neurotoxicology, 78, 11-20 (2020-02-12)
n-Hexane has been reported to induce serious peripheral neuropathy in workers. Pyrrole adducts are the unique reaction products of n-hexane in organisms and have been demonstrated to be critical to n-hexane neuropathy. Our previous studies have demonstrated that pyrrole adducts
Xianjie Li et al.
PloS one, 13(12), e0209939-e0209939 (2019-01-01)
Pyrrole adducts are specific reaction products of 2,5-hexadione (2,5-HD) in vivo and are considered highly relevant to the pathogenesis of peripheral nerve impairments after exposure to n-hexane, though the exact mechanism remains unclear. In this study, 40 male Wistar rats
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